Your donation will make a difference:
Cystic Fibrosis Trust
  • Home
  • /
  • Home
  • /
  • News
  • /
  • Worlds first newborn screening programme for CF

The pioneers behind the world's first newborn screening programme for CF

In the latest edition of CF Life, we shared Polly's story – the first baby in the world to be diagnosed with cystic fibrosis (CF) through an established newborn screening programme. She was born at Ipswich Hospital in East Anglia, which was the first region to set up a newborn screening service for CF, a model that was later adopted across the rest of the UK. We spoke to the pioneers behind the program, and looked at how their work has impacted people with CF and changed the way support is provided to families.

A time of transformative breakthroughs

Drs Mary and Anthony Heeley, Mary wearing a black jumper with a flowery scarf and Anthony in a grey shirtwith a pink collar undearneathDrs Anthony and Mary Heeley are both retired clinical biochemists with a special interest in inborn errors of metabolism (rare genetic or inherited disorders, like cystic fibrosis). The doctors, who have been married for 57 years, met when they were working in neighbouring labs as research fellows in London. They were the pioneers behind the world’s first regional screening programme for CF, established in 1980 in East Anglia.

The importance of early diagnosis for babies with CF was first recognised by Dr Harry Schwachman, a paediatrician at Boston Children’s Hospital in the 1950s. He realised this would provide the best possible outcome for children to receive the necessary support they needed. However, at the time, no neonatal screening test had been developed.

Anthony recalls, “There had been a screening test before immunoreactive trypsin (IRT) [the test used to screen for CF in newborn infants] which was undertaken by midwives in the delivery ward or at home. It measured pancreatic insufficiency, but many CF infants were born without pancreatic involvement so there was a huge population that were not detectable by screening. So, our task in the lab was to prove that there was a screening test that would detect all cases of cystic fibrosis.

“By the time the laboratory had moved from Cambridge to Peterborough in 1976, we had got into the second phase of newborn screening, which was for congenital hypothyroidism. For this we had to deal with a difficult technology for use with dried blood spots, and this experience was singularly important for what followed.

“In 1979, a paediatrician rushed into the lab with a report from researchers in New Zealand who had been measuring the pancreatic protein trypsin in the blood of CF newborns. They had found, to their surprise, that trypsin was actually elevated in the blood of CF newborns. We were very fast out of the trap following this up, and with some research funding, followed by support from the Cystic Fibrosis Trust, we got the first regional newborn screening service going in early 1980.”

“The funding from the Trust was very, very important,” says Mary. “In fact, it would not have got off the ground without the support.”

Better support for families

Group picture of Drs Anthony and Mary Heeley, Dr Jim Gould, Polly Crosby, and Dr Jacqui CalvinIt was through this newborn screening that Polly was diagnosed with CF – the first baby to officially be diagnosed through an established screening programme.

“I consider myself lucky,” she reflects in her feature for CF Life . “If I had been born a hundred years earlier, my illness would not have had a name, let alone a treatment of any kind. “Knowing that I had CF, pretty much from birth, meant that it was just a part of my life. It meant that my parents could put into place everything they possibly could to ensure they looked after me in the best way possible.”

It also meant paediatricians like Dr Jim Gould – Polly’s childhood doctor – could offer better support to families at an early stage. “Experience from before the times of screening show that quite a few children did not survive their first birthday,” explains Jim. “That changed as diagnosis was made earlier – we could offer nutritional and physiotherapy support, and start the early use of antibiotics, and giving a relatively good prognosis became almost the norm.”

Campaign for UK-wide screening

Dr Anjay Pillai and Dr Anthony Heeley presenting at the 40th anniversary of newborn screening in East Anglia event

After East Anglia became the very first region in the UK to fund neonatal screening for CF, it took another 20 years for it to be rolled out across the rest of the country. In April 1996, the Trust launched a campaign for all babies to be tested for CF as part of the newborn screening programme. At the time, 80% of babies were not tested for CF, with only a small number of health authorities offering testing. A quarter of children were over 18 months old by the time they were diagnosed.

The CF community drove the campaign, writing to and meeting MPs, talking to the media and sharing their views through a major Trust survey. It was not until 2007 that an expanded screening programme was rolled out across the whole of the UK, but it has changed the way CF is understood and cared for forever.

Dr Anjay Pillai, Consultant in Paediatric Respiratory Medicine and director of the paediatric CF service at the Jenny Lind Children’s Hospital in East Anglia, says, “Before newborn screening, children were usually diagnosed later in the course of the illness, when they presented with symptoms. This screening now detects nearly 97% of cases within two weeks of birth and provides an opportunity for early intervention and preventing complications. Together with specialist multi-disciplinary care and multiple medical advances, this has significantly improved outcomes and markedly enhanced life expectancy for people with cystic fibrosis.”

Dr Anjay and his CF team celebrated the 40th anniversary of the newborn screening service for CF in March, holding a momentous event for around 100 delegates and a panel of expert speakers who reflected on the past, present and future care and newborn screening.

You can read Polly's story 'A lucky life' in our latest edition of CF Life, or watch her story on YouTube.

Related content

  • Triple timeline announced by NICE

    Yesterday, NICE announced its planned timelines for assessing the triple combination therapy, with 16 December 2020 the date they expect to publish...

  • Emma's story: Getting the COVID-19 vaccine

    How has the past year been for you? Like everyone else who has CF, I had to shield from mid-February to August, before going back to work until...

  • UK CF Medical Association's statement on coronavirus

    If you have questions that are not answered in the below please contact our Helpline on While we endeavour to...

  • UK Cystic Fibrosis Registry

    How does the Registry work? CF care teams enter data at every specialist centre and clinic across the UK, with over 99% of people with CF consenting...